B Braun Medical recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include model 490:04046964186042.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical is recalling certain IV administration sets used with gravity and pump systems because they can cause medication to flow backward into the main IV line and fail to prime properly. This could lead to incorrect dosing or infections if the IV system is not functioning correctly.
The IV sets can allow medication from a secondary (piggyback) container to flow back into the primary IV container. This can cause incorrect dosing or contamination if the set cannot be properly primed to check for blockages.
Healthcare professionals using gravity IV systems or pump systems with these specific IV sets are most at risk. Patients receiving IV treatments with the recalled sets could face incorrect medication dosing or infection.
Check for the model number 490067 on the IV set label or the UDI-DI code 04046964186042. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Look for the model number 490067 or UDI-DI code 04046964186042 on the IV set label.
Reach out to B Braun Medical for guidance on whether your set is affected and next steps.
The model number is 490067 with UDI-DI code 04046964186042.
The recall affects IV sets used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check the label for model number 490067 or UDI-DI code 04046964186042. These sets were sold with specific B Braun pumps.
We’ve drafted a message you can send B Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0645-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0645-2026 from B Braun Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
